A 4.7-kb region of DNA sequence contained at the right end of the myxoma virus EcoRI-G2 fragment located 24 kb from the right end of the 163-kb genome has been determined. This region of the myxoma virus genome encodes homologs of the vaccinia virus genes A51R, A52R, A55R, A56R, and B1R; the myxoma virus gene equivalents have been given the prefix M. The MA55 gene encodes a
protein belonging to the kelch family of
actin-binding proteins, while the MA56 gene encodes a member of the
immunoglobulin superfamily related to a variety of cellular receptors and adhesion molecules. A novel myxoma virus early gene, MST3N, is a member of the eukaryotic
sialyltransferase gene family located between genes MA51 and MA52.
Detergent lysates prepared from myxoma virus-infected cell cultures contained a virally encoded
sialyltransferase activity that catalyzed the transfer of
sialic acid (Sia) from
CMP-Sia to an
asialofetuin glycoprotein acceptor. Analysis of the in vitro-sialylated
glycoprotein acceptor by digestion with
N-glycosidase F and by
lectin binding suggested that the MST3N gene encodes an
enzyme with Galbeta1,3(4)GlcNAc alpha2,3-sialyltransferase specificity for the N-linked
oligosaccharide of
glycoprotein.
Lectin binding assays demonstrated that alpha2,3-sialyltransferase activity is expressed by several known leporipoxviruses that naturally infect Sylvilagus rabbits. The
sialyltransferase is nonessential for myxoma virus replication in cell culture; however, disruption of the MST3N gene caused attenuation in vivo. The possible implications of the myxoma virus-expressed
sialyltransferase in terms of the host's defenses against
infection are discussed.